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Ruth Ottman

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TOP 3
Elan D Louis; Ruth Ottman; Nora Hernandez; Iuliana Ionita-Laza; Lorraine N Clark
Does rate of progression run in essential tremor families? Slower vs. faster progressors.
Elan D Louis; Ruth Ottman; Dennis J Tirri; Roy N Alcalay; Nora Hernandez; Lorraine N Clark
Prevalence and features of unreported dystonia in a family study of "pure" essential tremor.
Erin L Heinzen; Linda K Hong; Aatif M Husain; Jessica M Maia; Mark McCormack; James O McNamara; Mohamad A Mikati; Anna C Need; Gerard D O'Conner; Ruth Ottman; Ram S Puranam; Rodney A Radtke; Elizabeth K Ruzzo; Kevin V Shianna; Saurabh R Sinha; Sanjay M Sisodiya; Nicole M Walley; Qian Zhao; C Ryan Campbell; Gianpiero L Cavalleri; Krishna Chinthapalli; Elizabeth T Cirulli; Kenneth D Cronin; Norman Delanty; Chantal Depondt; William B Gallentine; Dongliang Ge; Curtis Gumbs; Min He; David B Goldstein
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.

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All Publications

2013: Elan D Louis; Ruth Ottman; Nora Hernandez; Iuliana Ionita-Laza; Lorraine N Clark
Does rate of progression run in essential tremor families? Slower vs. faster progressors.
Parkinsonism & related disorders 2013;19(3):363-6.
2013: Elan D Louis; Ruth Ottman; Dennis J Tirri; Roy N Alcalay; Nora Hernandez; Lorraine N Clark
Prevalence and features of unreported dystonia in a family study of "pure" essential tremor.
Parkinsonism & related disorders 2013;19(3):359-62.
2012: Erin L Heinzen; Linda K Hong; Aatif M Husain; Jessica M Maia; Mark McCormack; James O McNamara; Mohamad A Mikati; Anna C Need; Gerard D O'Conner; Ruth Ottman; Ram S Puranam; Rodney A Radtke; Elizabeth K Ruzzo; Kevin V Shianna; Saurabh R Sinha; Sanjay M Sisodiya; Nicole M Walley; Qian Zhao; C Ryan Campbell; Gianpiero L Cavalleri; Krishna Chinthapalli; Elizabeth T Cirulli; Kenneth D Cronin; Norman Delanty; Chantal Depondt; William B Gallentine; Dongliang Ge; Curtis Gumbs; Min He; David B Goldstein
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
American journal of human genetics 2012;91(2):293-302.
2011: Sara Shostak; Dana Zarhin; Ruth Ottman
What's at stake? Genetic information from the perspective of people with epilepsy and their family members.
Social science & medicine (1982) 2011;73(5):645-54.
2011: Ruth Ottman; richard lipton; Alan B Ettinger; Joyce A Cramer; Michael L Reed; Alan Morrison; George J Wan
Comorbidities of epilepsy: results from the Epilepsy Comorbidities and Health (EPIC) survey.
Epilepsia 2011;52(2):308-15.
2011: Ruth Ottman; Christie Barker-Cummings; C L Leibson; V M Vasoli; W Allen Hauser; Jeffrey R Buchhalter
Accuracy of family history information on epilepsy and other seizure disorders.
Neurology 2011;76(4):390-6.
2011: Ann M Madsen; Ruth Ottman; Susan E Hodge
Causal models for investigating complex genetic disease: II. what causal models can tell us about penetrance for additive, heterogeneity, and multiplicative two-locus models.
Human heredity 2011;72(1):63-72.
2011: Ann M Madsen; Susan E Hodge; Ruth Ottman
Causal models for investigating complex disease: I. A primer.
Human heredity 2011;72(1):54-62.
2010: Kimberly Pelak; Kevin V Shianna; Dongliang Ge; Jessica M Maia; Mingfu Zhu; Jason P Smith; Elizabeth T Cirulli; Jacques Fellay; Samuel P Dickson; Curtis E Gumbs; Erin L Heinzen; Anna C Need; Elizabeth K Ruzzo; Abanish Singh; C Ryan Campbell; Linda K Hong; Katharina A Lornsen; Alexander M McKenzie; Nara L M Sobreira; Julie E Hoover-Fong; Joshua D Milner; Ruth Ottman; Barton F Haynes; James J Goedert; David B Goldstein
The characterization of twenty sequenced human genomes.
PLoS genetics 2010;6(9):.
2010: Gary A Heiman; Kay Kamberakis; Richard Gill; Sergey Kalachikov; Timothy A Pedley; W Allen Hauser; Ruth Ottman
Evaluation of depression risk in LGI1 mutation carriers.
Epilepsia 2010;51(9):1685-90.
2010: Shanlee M Davis; Slavica K Katusic; William J Barbaresi; Jill Killian; Amy L Weaver; Ruth Ottman; Elaine C Wirrell
Epilepsy in children with attention-deficit/hyperactivity disorder.
Pediatric neurology 2010;42(5):325-30.
2010: Ruth Ottman; Shinichi Hirose; Satish Jain; Holger Lerche; Iscia Lopes-Cendes; Jeffrey L Noebels; José Serratosa; Federico Zara; Ingrid E Scheffer
Genetic testing in the epilepsies--report of the ILAE Genetics Commission.
Epilepsia 2010;51(4):655-70.
2010: Elan D Louis; O Dogu; Ruth Ottman
Subclinical tremor in normal controls with versus without a family history of essential tremor: data from the United States and Turkey.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2010;17(4):607-11.
2010: Ruth Ottman; Christie Barker-Cummings; Cynthia L Leibson; Vincent M Vasoli; W Allen Hauser; Jeffrey R Buchhalter
Validation of a brief screening instrument for the ascertainment of epilepsy.
Epilepsia 2010;51(2):191-7.
2009: A Poduri; Yuanjia Wang; D Gordon; S Barral-Rodriguez; Christie Barker-Cummings; A Ulgen; V Chitsazzadeh; R S Hill; N Risch; W Allen Hauser; Timothy A Pedley; Christopher Walsh; Ruth Ottman
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.
Neurology 2009;73(16):1264-72.
2008: Ruth Ottman; L Rosenberger; A Bagic; K Kamberakis; EVA RITZL; A M Wohlschlager; S Shamim; S Sato; C Liew; W D Gaillard; E Wiggs; M M Berl; P Reeves-Tyer; E H Baker; John A Butman; W H Theodore
Altered language processing in autosomal dominant partial epilepsy with auditory features.
Neurology 2008;71(24):1973-80.
2008: Peter Kinirons; daniel rabinowitz; Micheline Gravel; James Long; Melodie Winawer; Geneviève Sénéchal; Ruth Ottman; Patrick Cossette
Phenotypic concordance in 70 families with IGE-implications for genetic studies of epilepsy.
Epilepsy research 2008;82(1):21-28.
2008: Michael J Rosanoff; Ruth Ottman
Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
Neurology 2008;71(8):567-71.
2008: Yuanjia Wang; Lorraine N Clark; Elan D Louis; Helen Mejia-Santana; Juliette Harris; Lucien J Cote; Cheryl Waters; Howard Andrews; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman; daniel rabinowitz; Karen Marder
Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method.
Archives of neurology 2008;65(4):467-74.
2007: Elan D Louis; Julián Benito-León; Ruth Ottman; Félix Bermejo-Pareja
A population-based study of mortality in essential tremor.
Neurology 2007;69(21):1982-9.
2007: Lorraine N Clark; B M Ross; Yuanjia Wang; Helen Mejia-Santana; Juliette Harris; Elan D Louis; Lucien J Cote; Howard Andrews; Stanley Fahn; Cheryl Waters; Blair Ford; Steven Frucht; Ruth Ottman; Karen Marder
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease.
Neurology 2007;69(12):1270-7.
2007: Lorraine N Clark; Eneli Haamer; Helen Mejia-Santana; Juliette Harris; Suzanne Lesage; Alexandra Durr; Sabine Janin Bs; Katja Hedrich; Elan D Louis; Lucien J Cote; Howard Andrews; Stanley Fahn; Cheryl Waters; Blair Ford; Steven Frucht; William Scott; Christine Klein; Alexis Brice; Hanno Roomere; Ruth Ottman; Karen Marder
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.
Movement disorders : official journal of the Movement Disorder Society 2007;22(7):932-7.
2007: Gary A Heiman; Ruth Ottman; Rachel Saunders-Pullman; Laurie J Ozelius; Neil J Risch; Susan Bressman
Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(3):361-4.
2006: Yuanjia Wang; Ruth Ottman; daniel rabinowitz
A method for estimating penetrance from families sampled for linkage analysis.
Biometrics 2006;62(4):1081-8.
2006: Lorraine N Clark; Yuanjia Wang; Eric Karlins; L Saito; Helen Mejia-Santana; Juliette Harris; Elan D Louis; Lucien J Cote; Howard Andrews; Stanley Fahn; Cheryl Waters; Blair Ford; Steven Frucht; Ruth Ottman; Karen Marder
Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.
Neurology 2006;67(10):1786-91.
2006: Elan D Louis; Ruth Ottman
Study of possible factors associated with age of onset in essential tremor.
Movement disorders : official journal of the Movement Disorder Society 2006;21(11):1980-6.
2006: Sara Shostak; Ruth Ottman
Ethical, legal, and social dimensions of epilepsy genetics.
Epilepsia 2006;47(10):1595-602.
2006: H Choi; Melodie R Winawer; Sergey Kalachikov; Timothy A Pedley; W Allen Hauser; Ruth Ottman
Classification of partial seizure symptoms in genetic studies of the epilepsies.
Neurology 2006;66(11):1648-53.
2006: Lorraine N Clark; Shehla Afridi; Eric Karlins; Yuanjia Wang; Helen Mejia-Santana; Juliette Harris; Elan D Louis; Lucien J Cote; Howard Andrews; Stanley Fahn; Cheryl Waters; Blair Ford; Steven Frucht; Ruth Ottman; Karen Marder
Case-control study of the parkin gene in early-onset Parkinson disease.
Archives of neurology 2006;63(4):548-52.
2005: Melodie R Winawer; Carla Marini; Bronwyn E Grinton; daniel rabinowitz; Samuel F Berkovic; Ingrid E Scheffer; Ruth Ottman
Familial clustering of seizure types within the idiopathic generalized epilepsies.
Neurology 2005;65(4):523-8.
2005: Danielle Majoor-Krakauer; Paul G H Mulder; Lewis P Rowland; Ruth Ottman
A link between ALS and short residence on Guam.
Neurology 2005;64(10):1819-20.
2005: Ethel S Siris; Ruth Ottman; Edith Flaster; Jennifer L Kelsey
Familial aggregation of Paget's disease of bone. 1991.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2005;20(3):542-7.
2005: Ruth Ottman; Karina Berenson; Christie Barker-Cummings
Recruitment of families for genetic studies of epilepsy.
Epilepsia 2005;46(2):290-7.
2005: Ruth Ottman
Analysis of genetically complex epilepsies.
Epilepsia 2005;46 Suppl 10():7-14.
2005: Lorraine N Clark; Angelique Nicolai; Shehla Afridi; Juliette Harris; Helen Mejia-Santana; Lisa J Strug; Lucien J Cote; Elan D Louis; Howard Andrews; Cheryl Waters; Blair Ford; Steven Frucht; Stanley Fahn; Richard Mayeux; Ruth Ottman; Karen Marder
Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity.
Movement disorders : official journal of the Movement Disorder Society 2005;20(1):100-3.
2004: Gary A Heiman; Ruth Ottman; Rachel Saunders-Pullman; Laurie J Ozelius; Neil J Risch; Susan Bressman
Increased risk for recurrent major depression in DYT1 dystonia mutation carriers.
Neurology 2004;63(4):631-7.
2004: Dolores Garcia Arocena; Elan D Louis; Flora Tassone; T Conrad Gilliam; Ruth Ottman; Sébastien Jacquemont; Paul J Hagerman
Screen for expanded FMR1 alleles in patients with essential tremor.
Movement disorders : official journal of the Movement Disorder Society 2004;19(8):930-3.
2004: Gilberto Levy; Elan D Louis; Helen Mejia-Santana; Lucien J Cote; Howard Andrews; Juliette Harris; Cheryl Waters; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman; Karen Marder
Lack of familial aggregation of Parkinson disease and Alzheimer disease.
Archives of neurology 2004;61(7):1033-9.
2004: Lorraine N Clark; Shehla Afridi; Helen Mejia-Santana; Juliette Harris; Elan D Louis; Lucien J Cote; Howard Andrews; Andrew Singleton; Fabienne Wavrant De-Vrieze; John Hardy; Richard Mayeux; Stanley Fahn; Cheryl Waters; Blair Ford; Steven Frucht; Ruth Ottman; Karen Marder
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
Movement disorders : official journal of the Movement Disorder Society 2004;19(7):796-800.
2004: Ruth Ottman; Melodie R Winawer; Sergey Kalachikov; Christie Barker-Cummings; T Conrad Gilliam; Timothy A Pedley; W Allen Hauser
LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
Neurology 2004;62(7):1120-6.
2003: Melodie R Winawer; daniel rabinowitz; Timothy A Pedley; W Allen Hauser; Ruth Ottman
Genetic influences on myoclonic and absence seizures.
Neurology 2003;61(11):1576-81.
2003: Elan D Louis; Gilberto Levy; Helen Mejia-Santana; Lucien J Cote; Howard Andrews; Juliette Harris; Cheryl Waters; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman; Karen Marder
Risk of action tremor in relatives of tremor-dominant and postural instability gait disorder PD.
Neurology 2003;61(7):931-6.
2003: Karen Marder; Gilberto Levy; Elan D Louis; Helen Mejia-Santana; Lucien J Cote; Howard Andrews; Juliette Harris; Cheryl Waters; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman
Familial aggregation of early- and late-onset Parkinson's disease.
Annals of neurology 2003;54(4):507-13.
2003: Melodie R Winawer; daniel rabinowitz; Christie Barker-Cummings; Mark L Scheuer; Timothy A Pedley; W Allen Hauser; Ruth Ottman
Evidence for distinct genetic influences on generalized and localization-related epilepsy.
Epilepsia 2003;44(9):1176-82.
2003: Karen Marder; Gilberto Levy; Elan D Louis; Helen Mejia-Santana; Lucien J Cote; Howard Andrews; Juliette Harris; Cheryl Waters; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman
Accuracy of family history data on Parkinson's disease.
Neurology 2003;61(1):18-23.
2002: Nikolaos Scarmeas; T Shih; Yaakov Stern; Ruth Ottman; Lewis P Rowland
Premorbid weight, body mass, and varsity athletics in ALS.
Neurology 2002;59(5):773-5.
2002: Melodie R Winawer; Ruth Ottman; daniel rabinowitz
Concordance of disease form in kindreds ascertained through affected individuals.
Statistics in medicine 2002;21(13):1887-97.
2002: Sergey Kalachikov; Oleg V Evgrafov; Barbara Ross; Melodie R Winawer; Christie Barker-Cummings; Filippo Martinelli Boneschi; Chang Choi; Pavel Morozov; Kamna Das; Elita Teplitskaya; Andrew Yu; Eftihia Cayanis; Graciela Penchaszadeh; Andreas Kottmann; Timothy A Pedley; W Allen Hauser; Ruth Ottman; T Conrad Gilliam
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
Nature genetics 2002;30(3):335-41.
2002: Melodie R Winawer; Filippo Martinelli Boneschi; Christie Barker-Cummings; Joseph Lee; Jianjun Liu; Constantine Mekios; T Conrad Gilliam; Timothy A Pedley; W Allen Hauser; Ruth Ottman
Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.
Epilepsia 2002;43(1):60-7.
2001: Nicole Schupf; Ruth Ottman
Risk of epilepsy in offspring of affected women: association with maternal spontaneous abortion.
Neurology 2001;57(9):1642-9.
2001: Elan D Louis; Blair Ford; Steven Frucht; Ruth Ottman
Mild tremor in relatives of patients with essential tremor: what does this tell us about the penetrance of the disease?
Archives of neurology 2001;58(10):1584-9.
2001: Nicole Schupf; D Kapell; B Nightingale; Joseph Lee; J Mohlenhoff; S Bewley; Ruth Ottman; Richard Mayeux
Specificity of the fivefold increase in AD in mothers of adults with Down syndrome.
Neurology 2001;57(6):979-84.
2001: Elan D Louis; Blair Ford; Steven Frucht; daniel rabinowitz; Ruth Ottman
Evidence for familial aggregation of tremor in normal individuals.
Neurology 2001;57(1):110-4.
2001: Elan D Louis; Blair Ford; Steven Frucht; LF Barnes; M X-Tang; Ruth Ottman
Risk of tremor and impairment from tremor in relatives of patients with essential tremor: a community-based family study.
Annals of neurology 2001;49(6):761-9.
2001: Elan D Louis; LF Barnes; Blair Ford; Ruth Ottman
Family history information on essential tremor: potential biases related to the source of the cases.
Movement disorders : official journal of the Movement Disorder Society 2001;16(2):320-4.
2001: Ruth Ottman
Progress in the genetics of the partial epilepsies.
Epilepsia 2001;42 Suppl 5():24-30.
2000: Melodie R Winawer; Ruth Ottman; W Allen Hauser; Timothy A Pedley
Autosomal dominant partial epilepsy with auditory features: defining the phenotype.
Neurology 2000;54(11):2173-6.
2000: Gayatri Devi; Ruth Ottman; Ming-Xin Tang; Karen Marder; Yaakov Stern; Richard Mayeux
Familial aggregation of Alzheimer disease among whites, African Americans, and Caribbean Hispanics in northern Manhattan.
Archives of neurology 2000;57(1):72-7.
1999: Gayatri Devi; Ruth Ottman; Ming-Xin Tang; Karen Marder; Yaakov Stern; Benjamin Tycko; Richard Mayeux
Influence of APOE genotype on familial aggregation of AD in an urban population.
Neurology 1999;53(4):789-94.
1999: Elan D Louis; Blair Ford; KJ Wendt; Ruth Ottman
Validity of family history data on essential tremor.
Movement disorders : official journal of the Movement Disorder Society 1999;14(3):456-61.
1998: Ruth Ottman; Joseph Lee; W Allen Hauser; N Risch
Are generalized and localization-related epilepsies genetically distinct?
Archives of neurology 1998;55(3):339-44.
1998: Elan D Louis; Ruth Ottman; W Allen Hauser
How common is the most common adult movement disorder? estimates of the prevalence of essential tremor throughout the world.
Movement disorders : official journal of the Movement Disorder Society 1998;13(1):5-10.
1997: Nicole Schupf; Ruth Ottman
Reproduction among individuals with idiopathic/cryptogenic epilepsy: risk factors for spontaneous abortion.
Epilepsia 1997;38(7):824-9.
1997: Ruth Ottman; W Allen Hauser; Christie Barker-Cummings; Joseph Lee; N Risch
Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results.
American journal of human genetics 1997;60(3):667-75.
1997: Elan D Louis; Ruth Ottman; Blair Ford; Seth L Pullman; M Martinez; Stanley Fahn; W Allen Hauser
The Washington Heights-Inwood Genetic Study of Essential Tremor: methodologic issues in essential-tremor research.
Neuroepidemiology 1997;16(3):124-33.
1996: Ruth Ottman
Gene-environment interaction: definitions and study designs.
Preventive medicine 1996;25(6):764-70.
1996: Ruth Ottman; richard lipton
Is the comorbidity of epilepsy and migraine due to a shared genetic susceptibility?
Neurology 1996;47(4):918-24.
1996: Nicole Schupf; Ruth Ottman
Reproduction among individuals with idiopathic/cryptogenic epilepsy: risk factors for reduced fertility in marriage.
Epilepsia 1996;37(9):833-40.
1996: Elan D Louis; Ruth Ottman
How familial is familial tremor? The genetic epidemiology of essential tremor.
Neurology 1996;46(5):1200-5.
1996: Ruth Ottman; John F Annegers; N Risch; W A Hauser; M Susser
Relations of genetic and environmental factors in the etiology of epilepsy.
Annals of neurology 1996;39(4):442-9.
1996: Ruth Ottman; Joseph Lee; N Risch; W A Hauser; M Susser
Clinical indicators of genetic susceptibility to epilepsy.
Epilepsia 1996;37(4):353-61.
1995: Ruth Ottman; N Risch; W A Hauser; Timothy A Pedley; Joseph Lee; C Barker-Cummings; A Lustenberger; K J Nagle; K S Lee; Mark L Scheuer
Localization of a gene for partial epilepsy to chromosome 10q.
Nature genetics 1995;10(1):56-60.
1995: Richard Mayeux; Ruth Ottman; G Maestre; Colleen Ngai; Ming-Xin Tang; Henry N Ginsberg; M Chun; Benjamin Tycko; Michael L. Shelanski
Synergistic effects of traumatic head injury and apolipoprotein-epsilon 4 in patients with Alzheimer's disease.
Neurology 1995;45(3 Pt 1):555-7.
1995: G Maestre; Ruth Ottman; Yaakov Stern; Barry Gurland; M Chun; Ming-Xin Tang; Michael L. Shelanski; Benjamin Tycko; Richard Mayeux
Apolipoprotein E and Alzheimer's disease: ethnic variation in genotypic risks.
Annals of neurology 1995;37(2):254-9.
1994: M C Paik; W Y Tsai; Ruth Ottman
Multivariate survival analysis using piecewise gamma frailty.
Biometrics 1994;50(4):975-88.
1994: Ruth Ottman; richard lipton
Comorbidity of migraine and epilepsy.
Neurology 1994;44(11):2105-10.
1994: D Majoor-Krakauer; Ruth Ottman; William G Johnson; Lewis P Rowland
Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility.
Neurology 1994;44(10):1872-7.
1994: Nicole Schupf; Ruth Ottman
Likelihood of pregnancy in individuals with idiopathic/cryptogenic epilepsy: social and biologic influences.
Epilepsia 1994;35(4):750-6.
1993: Ruth Ottman; Joseph Lee; W A Hauser; S Hong; D Hesdorffer; Nicole Schupf; Timothy A Pedley; Mark L Scheuer
Reliability of seizure classification using a semistructured interview.
Neurology 1993;43(12):2526-30.
1993: Richard Mayeux; Yaakov Stern; Ruth Ottman; TK Tatemichi; Ming-Xin Tang; G Maestre; Colleen Ngai; Benjamin Tycko; Henry N Ginsberg
The apolipoprotein epsilon 4 allele in patients with Alzheimer's disease.
Annals of neurology 1993;34(5):752-4.
1993: Ruth Ottman; S Hong; richard lipton
Validity of family history data on severe headache and migraine.
Neurology 1993;43(10):1954-60.
1993: Ruth Ottman; W A Hauser; M Susser
Validity of family history data on seizure disorders.
Epilepsia 1993;34(3):469-75.
1993: Richard Mayeux; Ruth Ottman; Ming-Xin Tang; L Noboa-Bauza; Karen Marder; Barry Gurland; Yaakov Stern
Genetic susceptibility and head injury as risk factors for Alzheimer's disease among community-dwelling elderly persons and their first-degree relatives.
Annals of neurology 1993;33(5):494-501.
1991: Ruth Ottman; John F Annegers; L T Kurland
Familial aggregation and severity of epilepsy.
Epilepsia 1991;32(4):523-9.
1990: Ruth Ottman; W A Hauser; L Stallone
Semistructured interview for seizure classification: agreement with physicians' diagnoses.
Epilepsia 1990;31(1):110-5.
1989: Ruth Ottman; John F Annegers; W A Hauser; L T Kurland
Seizure risk in offspring of parents with generalized versus partial epilepsy.
Epilepsia 1989;30(2):157-61.
1989: Ruth Ottman
Genetics of the partial epilepsies: a review.
Epilepsia 1989;30(1):107-11.
1988: Ruth Ottman; J F Annegers; W A Hauser; L T Kurland
Higher risk of seizures in offspring of mothers than of fathers with epilepsy.
American journal of human genetics 1988;43(3):257-64.